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Select item 14915669371.

rs1491566937 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 18:70306477 (GRCh38)
18:67973713 (GRCh37)
Canonical SPDI:: NC_000018.10:70306476:CA:
Gene:: SOCS6 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.01442/171 (ALFA)
-=0.00386/109 (TOMMO)
HGVS:: NC_000018.10:g.70306477_70306478del, NC_000018.9:g.67973713_67973714del

Select item 14914893532.

rs1491489353 has merged into rs1306876861 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTT>-,T,TT,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 18:70310484 (GRCh38)
18:67977720 (GRCh37)
Canonical SPDI:: NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT
Gene:: SOCS6 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTTTT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.70310484_70310488del, NC_000018.10:g.70310485_70310488del, NC_000018.10:g.70310486_70310488del, NC_000018.10:g.70310487_70310488del, NC_000018.10:g.70310488del, NC_000018.10:g.70310488dup, NC_000018.10:g.70310487_70310488dup, NC_000018.10:g.70310486_70310488dup, NC_000018.10:g.70310485_70310488dup, NC_000018.10:g.70310484_70310488dup, NC_000018.10:g.70310483_70310488dup, NC_000018.10:g.70310469_70310488T[30]GTTTTTTTTTTTTTTTTTTTTT[1], NC_000018.10:g.70310469_70310488T[41]CTTTTTTTTTTTTTTTTTTTTTT[1], NC_000018.9:g.67977720_67977724del, NC_000018.9:g.67977721_67977724del, NC_000018.9:g.67977722_67977724del, NC_000018.9:g.67977723_67977724del, NC_000018.9:g.67977724del, NC_000018.9:g.67977724dup, NC_000018.9:g.67977723_67977724dup, NC_000018.9:g.67977722_67977724dup, NC_000018.9:g.67977721_67977724dup, NC_000018.9:g.67977720_67977724dup, NC_000018.9:g.67977719_67977724dup, NC_000018.9:g.67977705_67977724T[30]GTTTTTTTTTTTTTTTTTTTTT[1], NC_000018.9:g.67977705_67977724T[41]CTTTTTTTTTTTTTTTTTTTTTT[1]

Select item 14914320423.

rs1491432042 has merged into rs966328703 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTT>-,TTTT,TTTTT,TTTTTTT,TTTTTTTT [Show Flanks]
Chromosome:: 18:70310289 (GRCh38)
18:67977525 (GRCh37)
Canonical SPDI:: NC_000018.10:70310280:TTTTTTTTTTTTTT:TTTTTTTT,NC_000018.10:70310280:TTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000018.10:70310280:TTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000018.10:70310280:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000018.10:70310280:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT
Gene:: SOCS6 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTT=0./0 (ALFA)
-=0.000015/4 (TOPMED)
HGVS:: NC_000018.10:g.70310289_70310294del, NC_000018.10:g.70310293_70310294del, NC_000018.10:g.70310294del, NC_000018.10:g.70310294dup, NC_000018.10:g.70310293_70310294dup, NC_000018.9:g.67977525_67977530del, NC_000018.9:g.67977529_67977530del, NC_000018.9:g.67977530del, NC_000018.9:g.67977530dup, NC_000018.9:g.67977529_67977530dup

Select item 14913785614.

rs1491378561 [Homo sapiens]

Variant type:: SNV:
Alleles:: ->G
Chromosome:: no mapping
Canonical SPDI:

Select item 14913522405.

rs1491352240 has merged into rs375704179 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,T,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTCTTTTTTTTTTTTTTT,TTTTTTTTCTTTTTTTTTTTTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTATATATTAGATCTCTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 18:70296917 (GRCh38)
18:67964153 (GRCh37)
Canonical SPDI:: NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTATATATTAGATCTCTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70296906:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: SOCS6 (Varview)
Functional Consequence:: 5_prime_UTR_variant,genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000018.10:g.70296917_70296918del, NC_000018.10:g.70296918del, NC_000018.10:g.70296918dup, NC_000018.10:g.70296917_70296918dup, NC_000018.10:g.70296916_70296918dup, NC_000018.10:g.70296915_70296918dup, NC_000018.10:g.70296914_70296918dup, NC_000018.10:g.70296913_70296918dup, NC_000018.10:g.70296907_70296918T[18]CTTTTTTTTTTTTTTT[1], NC_000018.10:g.70296907_70296918T[18]CTTTTTTTTTTTTTTTTTT[1], NC_000018.10:g.70296912_70296918dup, NC_000018.10:g.70296911_70296918dup, NC_000018.10:g.70296910_70296918dup, NC_000018.10:g.70296909_70296918dup, NC_000018.10:g.70296908_70296918dup, NC_000018.10:g.70296907_70296918T[23]CTTTTTTTTTTTTTTTTTTT[1], NC_000018.10:g.70296907_70296918dup, NC_000018.10:g.70296918_70296919insTTTTTTTTTTTTT, NC_000018.10:g.70296918_70296919insTTTTTTTTTTTTTT, NC_000018.10:g.70296918_70296919insTTTTTTTTTTTTTTT, NC_000018.10:g.70296918_70296919insTTTTTTTTTTTTTTTT, NC_000018.10:g.70296918_70296919insTTTTTTTTTTTTTTTTT, NC_000018.10:g.70296918_70296919insTTTTTTTTTTTTTTTTTT, NC_000018.10:g.70296918_70296919insTTTTTTTTTTTTTTTTTTT, NC_000018.10:g.70296918_70296919insTTTTTTTTTTTTTTTTTTTT, NC_000018.10:g.70296918_70296919insTTTTTTTTTTTTTTTTTTTTT, NC_000018.10:g.70296918_70296919insTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.10:g.70296918_70296919insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.10:g.70296918_70296919insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.10:g.70296918_70296919insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.10:g.70296918_70296919insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.10:g.70296907_70296918T[41]AT[3]TAGATCTCTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000018.10:g.70296918_70296919insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.10:g.70296918_70296919insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.10:g.70296918_70296919insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.9:g.67964153_67964154del, NC_000018.9:g.67964154del, NC_000018.9:g.67964154dup, NC_000018.9:g.67964153_67964154dup, NC_000018.9:g.67964152_67964154dup, NC_000018.9:g.67964151_67964154dup, NC_000018.9:g.67964150_67964154dup, NC_000018.9:g.67964149_67964154dup, NC_000018.9:g.67964143_67964154T[18]CTTTTTTTTTTTTTTT[1], NC_000018.9:g.67964143_67964154T[18]CTTTTTTTTTTTTTTTTTT[1], NC_000018.9:g.67964148_67964154dup, NC_000018.9:g.67964147_67964154dup, NC_000018.9:g.67964146_67964154dup, NC_000018.9:g.67964145_67964154dup, NC_000018.9:g.67964144_67964154dup, NC_000018.9:g.67964143_67964154T[23]CTTTTTTTTTTTTTTTTTTT[1], NC_000018.9:g.67964143_67964154dup, NC_000018.9:g.67964154_67964155insTTTTTTTTTTTTT, NC_000018.9:g.67964154_67964155insTTTTTTTTTTTTTT, NC_000018.9:g.67964154_67964155insTTTTTTTTTTTTTTT, NC_000018.9:g.67964154_67964155insTTTTTTTTTTTTTTTT, NC_000018.9:g.67964154_67964155insTTTTTTTTTTTTTTTTT, NC_000018.9:g.67964154_67964155insTTTTTTTTTTTTTTTTTT, NC_000018.9:g.67964154_67964155insTTTTTTTTTTTTTTTTTTT, NC_000018.9:g.67964154_67964155insTTTTTTTTTTTTTTTTTTTT, NC_000018.9:g.67964154_67964155insTTTTTTTTTTTTTTTTTTTTT, NC_000018.9:g.67964154_67964155insTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.9:g.67964154_67964155insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.9:g.67964154_67964155insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.9:g.67964154_67964155insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.9:g.67964154_67964155insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.9:g.67964143_67964154T[41]AT[3]TAGATCTCTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000018.9:g.67964154_67964155insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.9:g.67964154_67964155insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000018.9:g.67964154_67964155insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047437942.1:c.-8620_-8619del, XM_047437942.1:c.-8619del, XM_047437942.1:c.-8619dup, XM_047437942.1:c.-8620_-8619dup, XM_047437942.1:c.-8621_-8619dup, XM_047437942.1:c.-8622_-8619dup, XM_047437942.1:c.-8623_-8619dup, XM_047437942.1:c.-8624_-8619dup, XM_047437942.1:c.-8630_-8619T[18]CTTTTTTTTTTTTTTT[1], XM_047437942.1:c.-8630_-8619T[18]CTTTTTTTTTTTTTTTTTT[1], XM_047437942.1:c.-8625_-8619dup, XM_047437942.1:c.-8626_-8619dup, XM_047437942.1:c.-8627_-8619dup, XM_047437942.1:c.-8628_-8619dup, XM_047437942.1:c.-8629_-8619dup, XM_047437942.1:c.-8630_-8619T[23]CTTTTTTTTTTTTTTTTTTT[1], XM_047437942.1:c.-8630_-8619dup, XM_047437942.1:c.-8619_-8618insTTTTTTTTTTTTT, XM_047437942.1:c.-8619_-8618insTTTTTTTTTTTTTT, XM_047437942.1:c.-8619_-8618insTTTTTTTTTTTTTTT, XM_047437942.1:c.-8619_-8618insTTTTTTTTTTTTTTTT, XM_047437942.1:c.-8619_-8618insTTTTTTTTTTTTTTTTT, XM_047437942.1:c.-8619_-8618insTTTTTTTTTTTTTTTTTT, XM_047437942.1:c.-8619_-8618insTTTTTTTTTTTTTTTTTTT, XM_047437942.1:c.-8619_-8618insTTTTTTTTTTTTTTTTTTTT, XM_047437942.1:c.-8619_-8618insTTTTTTTTTTTTTTTTTTTTT, XM_047437942.1:c.-8619_-8618insTTTTTTTTTTTTTTTTTTTTTTT, XM_047437942.1:c.-8619_-8618insTTTTTTTTTTTTTTTTTTTTTTTT, XM_047437942.1:c.-8619_-8618insTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047437942.1:c.-8619_-8618insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047437942.1:c.-8619_-8618insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047437942.1:c.-8630_-8619T[41]AT[3]TAGATCTCTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_047437942.1:c.-8619_-8618insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047437942.1:c.-8619_-8618insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047437942.1:c.-8619_-8618insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14913052406.

rs1491305240 has merged into rs1306876861 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTT>-,T,TT,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 18:70310484 (GRCh38)
18:67977720 (GRCh37)
Canonical SPDI:: NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTT,NC_000018.10:70310468:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTT
Gene:: SOCS6 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTTTT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.70310484_70310488del, NC_000018.10:g.70310485_70310488del, NC_000018.10:g.70310486_70310488del, NC_000018.10:g.70310487_70310488del, NC_000018.10:g.70310488del, NC_000018.10:g.70310488dup, NC_000018.10:g.70310487_70310488dup, NC_000018.10:g.70310486_70310488dup, NC_000018.10:g.70310485_70310488dup, NC_000018.10:g.70310484_70310488dup, NC_000018.10:g.70310483_70310488dup, NC_000018.10:g.70310469_70310488T[30]GTTTTTTTTTTTTTTTTTTTTT[1], NC_000018.10:g.70310469_70310488T[41]CTTTTTTTTTTTTTTTTTTTTTT[1], NC_000018.9:g.67977720_67977724del, NC_000018.9:g.67977721_67977724del, NC_000018.9:g.67977722_67977724del, NC_000018.9:g.67977723_67977724del, NC_000018.9:g.67977724del, NC_000018.9:g.67977724dup, NC_000018.9:g.67977723_67977724dup, NC_000018.9:g.67977722_67977724dup, NC_000018.9:g.67977721_67977724dup, NC_000018.9:g.67977720_67977724dup, NC_000018.9:g.67977719_67977724dup, NC_000018.9:g.67977705_67977724T[30]GTTTTTTTTTTTTTTTTTTTTT[1], NC_000018.9:g.67977705_67977724T[41]CTTTTTTTTTTTTTTTTTTTTTT[1]

Select item 14912620807.

rs1491262080 has merged into rs1214220274 [Homo sapiens]

Variant type:: DELINS
Alleles:: TA>-,TATA [Show Flanks]
Chromosome:: 18:70302761 (GRCh38)
18:67969997 (GRCh37)
Canonical SPDI:: NC_000018.10:70302750:TATATATATATA:TATATATATA,NC_000018.10:70302750:TATATATATATA:TATATATATATATA
Gene:: SOCS6 (Varview)
Functional Consequence:: 5_prime_UTR_variant,genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TATATATATATATA=0./0 (ALFA)
-=0.000142/2 (TOMMO)
-=0.00058/67 (GnomAD)
HGVS:: NC_000018.10:g.70302751TA[5], NC_000018.10:g.70302751TA[7], NC_000018.9:g.67969987TA[5], NC_000018.9:g.67969987TA[7], XM_047437942.1:c.-2786TA[5], XM_047437942.1:c.-2786TA[7]

Select item 14912552718.

rs1491255271 has merged into rs755917853 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>-,GTGT [Show Flanks]
Chromosome:: 18:70314887 (GRCh38)
18:67982123 (GRCh37)
Canonical SPDI:: NC_000018.10:70314885:TGT:T,NC_000018.10:70314885:TGT:TGTGT
Gene:: SOCS6 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by cluster
MAF:: -=0.000008/1 (GnomAD)
HGVS:: NC_000018.10:g.70314887_70314888del, NC_000018.10:g.70314887_70314888dup, NC_000018.9:g.67982123_67982124del, NC_000018.9:g.67982123_67982124dup

Select item 14912342559.

rs1491234255 has merged into rs55702216 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAA>-,AA,AAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 18:70306484 (GRCh38)
18:67973720 (GRCh37)
Canonical SPDI:: NC_000018.10:70306477:AAAAAAAAAAAAAAAAAAAAAA:AAAAAA,NC_000018.10:70306477:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000018.10:70306477:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000018.10:70306477:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000018.10:70306477:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000018.10:70306477:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000018.10:70306477:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000018.10:70306477:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000018.10:70306477:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000018.10:70306477:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000018.10:70306477:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000018.10:70306477:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000018.10:70306477:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000018.10:70306477:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000018.10:70306477:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000018.10:70306477:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000018.10:70306477:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000018.10:70306477:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000018.10:70306477:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000018.10:70306477:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000018.10:70306477:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000018.10:70306477:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000018.10:70306477:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: SOCS6 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAA=0./0 (ALFA)
HGVS:: NC_000018.10:g.70306484_70306499del, NC_000018.10:g.70306486_70306499del, NC_000018.10:g.70306487_70306499del, NC_000018.10:g.70306490_70306499del, NC_000018.10:g.70306491_70306499del, NC_000018.10:g.70306492_70306499del, NC_000018.10:g.70306493_70306499del, NC_000018.10:g.70306494_70306499del, NC_000018.10:g.70306495_70306499del, NC_000018.10:g.70306496_70306499del, NC_000018.10:g.70306497_70306499del, NC_000018.10:g.70306498_70306499del, NC_000018.10:g.70306499del, NC_000018.10:g.70306499dup, NC_000018.10:g.70306498_70306499dup, NC_000018.10:g.70306497_70306499dup, NC_000018.10:g.70306496_70306499dup, NC_000018.10:g.70306495_70306499dup, NC_000018.10:g.70306494_70306499dup, NC_000018.10:g.70306493_70306499dup, NC_000018.10:g.70306492_70306499dup, NC_000018.10:g.70306491_70306499dup, NC_000018.10:g.70306490_70306499dup, NC_000018.9:g.67973720_67973735del, NC_000018.9:g.67973722_67973735del, NC_000018.9:g.67973723_67973735del, NC_000018.9:g.67973726_67973735del, NC_000018.9:g.67973727_67973735del, NC_000018.9:g.67973728_67973735del, NC_000018.9:g.67973729_67973735del, NC_000018.9:g.67973730_67973735del, NC_000018.9:g.67973731_67973735del, NC_000018.9:g.67973732_67973735del, NC_000018.9:g.67973733_67973735del, NC_000018.9:g.67973734_67973735del, NC_000018.9:g.67973735del, NC_000018.9:g.67973735dup, NC_000018.9:g.67973734_67973735dup, NC_000018.9:g.67973733_67973735dup, NC_000018.9:g.67973732_67973735dup, NC_000018.9:g.67973731_67973735dup, NC_000018.9:g.67973730_67973735dup, NC_000018.9:g.67973729_67973735dup, NC_000018.9:g.67973728_67973735dup, NC_000018.9:g.67973727_67973735dup, NC_000018.9:g.67973726_67973735dup

Select item 149118135510.

rs1491181355 [Homo sapiens]

Variant type:: DEL
Alleles:: GT>- [Show Flanks]
Chromosome:: 18:70310280 (GRCh38)
18:67977516 (GRCh37)
Canonical SPDI:: NC_000018.10:70310279:GT:
Gene:: SOCS6 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000123/14 (GnomAD)
HGVS:: NC_000018.10:g.70310280_70310281del, NC_000018.9:g.67977516_67977517del

Select item 149102073211.

rs1491020732 has merged into rs1555790121 [Homo sapiens]

Variant type:: DELINS
Alleles:: GTGT>-,GT,GTGTGT [Show Flanks]
Chromosome:: 18:70314863 (GRCh38)
18:67982099 (GRCh37)
Canonical SPDI:: NC_000018.10:70314859:TGTGTGT:TGT,NC_000018.10:70314859:TGTGTGT:TGTGT,NC_000018.10:70314859:TGTGTGT:TGTGTGTGT
Gene:: SOCS6 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTGT=0./0 (ALFA)
TG=0.00018/5 (TOMMO)
HGVS:: NC_000018.10:g.70314861GT[1], NC_000018.10:g.70314861GT[2], NC_000018.10:g.70314861GT[4], NC_000018.9:g.67982097GT[1], NC_000018.9:g.67982097GT[2], NC_000018.9:g.67982097GT[4]

Select item 149099819812.

rs1490998198 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 18:70300991 (GRCh38)
18:67968227 (GRCh37)
Canonical SPDI:: NC_000018.10:70300990:T:C
Gene:: SOCS6 (Varview)
Functional Consequence:: 5_prime_UTR_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000018.10:g.70300991T>C, NC_000018.9:g.67968227T>C, XM_047437942.1:c.-4546T>C

Select item 149095491413.

rs1490954914 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:70324701 (GRCh38)
18:67991937 (GRCh37)
Canonical SPDI:: NC_000018.10:70324700:A:G
Gene:: SOCS6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0.000111/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000018.10:g.70324701A>G, NC_000018.9:g.67991937A>G, XM_005266783.5:c.33A>G, XM_005266783.4:c.33A>G, XM_005266783.3:c.33A>G, XM_005266783.2:c.33A>G, XM_005266783.1:c.33A>G, NM_004232.4:c.33A>G, NM_004232.3:c.33A>G, XM_017026087.2:c.33A>G, XM_017026087.1:c.33A>G, XM_017026086.2:c.33A>G, XM_017026086.1:c.33A>G, XM_047437942.1:c.33A>G, XM_047437941.1:c.33A>G, XM_047437939.1:c.33A>G, XM_047437937.1:c.33A>G, XM_047437940.1:c.33A>G, XM_047437938.1:c.33A>G

Select item 149093950514.

rs1490939505 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 18:70288205 (GRCh38)
18:67955441 (GRCh37)
Canonical SPDI:: NC_000018.10:70288204:T:C
Gene:: SOCS6 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000018.10:g.70288205T>C, NC_000018.9:g.67955441T>C

Select item 149092083115.

rs1490920831 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 18:70316064 (GRCh38)
18:67983300 (GRCh37)
Canonical SPDI:: NC_000018.10:70316063:G:C
Gene:: SOCS6 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000019/5 (TOPMED)
HGVS:: NC_000018.10:g.70316064G>C, NC_000018.9:g.67983300G>C

Select item 149088879816.

rs1490888798 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 18:70317182 (GRCh38)
18:67984418 (GRCh37)
Canonical SPDI:: NC_000018.10:70317181:T:C
Gene:: SOCS6 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000018.10:g.70317182T>C, NC_000018.9:g.67984418T>C

Select item 149088156717.

rs1490881567 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 18:70330270 (GRCh38)
18:67997506 (GRCh37)
Canonical SPDI:: NC_000018.10:70330269:T:C
Gene:: SOCS6 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000018.10:g.70330270T>C, NC_000018.9:g.67997506T>C

Select item 149084468818.

rs1490844688 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 18:70302005 (GRCh38)
18:67969241 (GRCh37)
Canonical SPDI:: NC_000018.10:70302004:G:A
Gene:: SOCS6 (Varview)
Functional Consequence:: 5_prime_UTR_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.70302005G>A, NC_000018.9:g.67969241G>A, XM_047437942.1:c.-3532G>A

Select item 149076816619.

rs1490768166 [Homo sapiens]

Variant type:: DELINS
Alleles:: ATT>- [Show Flanks]
Chromosome:: 18:70321640 (GRCh38)
18:67988876 (GRCh37)
Canonical SPDI:: NC_000018.10:70321637:TTATT:TT
Gene:: SOCS6 (Varview)
Functional Consequence:: intron_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000018.10:g.70321640_70321642del, NC_000018.9:g.67988876_67988878del, XM_047437939.1:c.-2135_-2133del

Select item 149076341220.

rs1490763412 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 18:70326758 (GRCh38)
18:67993994 (GRCh37)
Canonical SPDI:: NC_000018.10:70326757:C:T
Gene:: SOCS6 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000018.10:g.70326758C>T, NC_000018.9:g.67993994C>T, XM_005266783.5:c.*482C>T, XM_005266783.4:c.*482C>T, XM_005266783.3:c.*482C>T, XM_005266783.2:c.*482C>T, XM_005266783.1:c.*482C>T, NM_004232.4:c.*482C>T, NM_004232.3:c.*482C>T, XM_017026087.2:c.*482C>T, XM_017026087.1:c.*482C>T, XM_017026086.2:c.*482C>T, XM_017026086.1:c.*482C>T, XM_047437942.1:c.*482C>T, XM_047437941.1:c.*482C>T, XM_047437939.1:c.*482C>T, XM_047437937.1:c.*482C>T, XM_047437940.1:c.*482C>T, XM_047437938.1:c.*482C>T

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